Senior QA Associate: GMP, Artwork & Master Data

Real; Breda; On-site; EUR 60,000 - 75,000; Full time

Job summary

Real is seeking a Senior Associate Quality Assurance (QA) to support quality operations in Breda, Netherlands. This role focuses on GMP-compliant QA activities, SAP Master Data review, artwork approval, and SOP management within a regulated pharmaceutical manufacturing environment.

You will collaborate with Global Artwork Centre, Master Data, Regulatory Affairs, Supply Chain, SMEs, and QA leadership to deliver metrics and drive continuous improvement while ensuring patient safety and product

Qualifications

• 3 years of QA or pharmaceutical manufacturing experience.
• Knowledge of GMP, GDP and/or GCP regulations.
• Experience in a regulated pharmaceutical or medical device environment.
• Excellent English communication and meticulous attention to detail.

Responsibilities

• QA review and approval of SAP Master Data activities and documentation.
• Review and approve artwork for medicinal products.
• Ensure compliance with GMP and regulatory requirements.
• Maintain QA systems and support data integrity initiatives.
• Develop and monitor quality metrics and reports.
• Collaborate with cross-functional teams across QA leadership, Regulatory, and Supply Chain.

Skills

Quality Assurance

GMP knowledge

Documentation

Communication

Attention to detail

Prioritization

Education

Bachelor's degree in Life Sciences or related

Tools

SAP

SOP documentation

Quality systems

Job description

Real is seeking a Senior Associate Quality Assurance (QA) to support quality operations in Breda, Netherlands. This role focuses on GMP-compliant QA activities, SAP Master Data review, artwork approval, and SOP management within a regulated pharmaceutical manufacturing environment.

You will collaborate with Global Artwork Centre, Master Data, Regulatory Affairs, Supply Chain, SMEs, and QA leadership to deliver metrics and drive continuous improvement while ensuring patient safety and product